Diastereoselective Additions of Allylmetal Reagents to Free and Protected syn-α,β-Dihydroxyketones Enable Efficient Synthetic Routes to Methyl Trioxacarcinoside A-Reference-Cited by-同舟云学术

Diastereoselective Additions of Allylmetal Reagents to Free and Protected syn-α,β-Dihydroxyketones Enable Efficient Synthetic Routes to Methyl Trioxacarcinoside A

Published:2012-03-09 Issue:7 Volume:14 Page:1812-1815
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Smaltz Daniel J.¹,Švenda Jakub¹,Myers Andrew G.¹

Affiliation:

1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol300377a

Reference41 articles.

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4. Polyketomycin, a New Antibiotic from Streptomyces sp. MK277-AF1. I. Taxonomy, Production, Isolation, Physico-chemical Properties and Biological Activities.

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